ClinVar Miner

List of variants in gene SIGLEC11 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_052884.3(SIGLEC11):c.1860C>G (p.Ser620Arg) rs149680238 0.00024
NM_052884.3(SIGLEC11):c.2018T>G (p.Ile673Ser) rs201746673 0.00019
NM_052884.3(SIGLEC11):c.1343C>T (p.Ser448Phe) rs144054317 0.00014
NM_052884.3(SIGLEC11):c.284T>C (p.Val95Ala) rs568916513 0.00013
NM_052884.3(SIGLEC11):c.361G>A (p.Ala121Thr) rs376315578 0.00010
NM_052884.3(SIGLEC11):c.1072C>G (p.Leu358Val) rs147064231 0.00008
NM_052884.3(SIGLEC11):c.290T>C (p.Met97Thr) rs753065493 0.00008
NM_052884.3(SIGLEC11):c.1579G>A (p.Gly527Ser) rs138849107 0.00007
NM_052884.3(SIGLEC11):c.1819C>A (p.Pro607Thr) rs1047234518 0.00007
NM_052884.3(SIGLEC11):c.1316A>G (p.Gln439Arg) rs369288400 0.00006
NM_052884.3(SIGLEC11):c.178C>T (p.Arg60Trp) rs556232816 0.00005
NM_052884.3(SIGLEC11):c.154G>A (p.Val52Met) rs574890050 0.00004
NM_052884.3(SIGLEC11):c.1510G>A (p.Glu504Lys) rs759718197 0.00003
NM_052884.3(SIGLEC11):c.1531G>A (p.Gly511Arg) rs569790579 0.00003
NM_052884.3(SIGLEC11):c.1615G>A (p.Gly539Arg) rs767478430 0.00003
NM_052884.3(SIGLEC11):c.1877C>T (p.Pro626Leu) rs368679072 0.00003
NM_052884.3(SIGLEC11):c.230G>A (p.Arg77Gln) rs748856612 0.00003
NM_052884.3(SIGLEC11):c.1223A>G (p.Gln408Arg) rs780898655 0.00002
NM_052884.3(SIGLEC11):c.125T>G (p.Val42Gly) rs201377938 0.00002
NM_052884.3(SIGLEC11):c.1573A>G (p.Ser525Gly) rs988238286 0.00002
NM_052884.3(SIGLEC11):c.1610T>C (p.Val537Ala) rs777794233 0.00002
NM_052884.3(SIGLEC11):c.676C>T (p.Leu226Phe) rs764395821 0.00002
NM_052884.3(SIGLEC11):c.1516A>T (p.Thr506Ser) rs749874555 0.00001
NM_052884.3(SIGLEC11):c.1852G>A (p.Ala618Thr) rs200595712 0.00001
NM_052884.3(SIGLEC11):c.1892C>G (p.Thr631Ser) rs374770988 0.00001
NM_052884.3(SIGLEC11):c.415G>A (p.Val139Met) rs751895660 0.00001
NM_052884.3(SIGLEC11):c.515C>T (p.Pro172Leu) rs779205214 0.00001
NM_052884.3(SIGLEC11):c.737G>A (p.Arg246His) rs1253286759 0.00001
NM_052884.3(SIGLEC11):c.991C>T (p.Arg331Cys) rs769673458 0.00001
NM_052884.3(SIGLEC11):c.1004G>A (p.Arg335Gln)
NM_052884.3(SIGLEC11):c.103A>G (p.Ser35Gly) rs2514941697
NM_052884.3(SIGLEC11):c.1055A>T (p.Gln352Leu) rs751178318
NM_052884.3(SIGLEC11):c.1070A>C (p.Asn357Thr)
NM_052884.3(SIGLEC11):c.1093G>A (p.Ala365Thr) rs2514931732
NM_052884.3(SIGLEC11):c.1111G>A (p.Glu371Lys) rs2514930791
NM_052884.3(SIGLEC11):c.1118T>G (p.Leu373Arg)
NM_052884.3(SIGLEC11):c.1125C>A (p.Asn375Lys) rs374104181
NM_052884.3(SIGLEC11):c.1126G>A (p.Gly376Ser) rs142292396
NM_052884.3(SIGLEC11):c.1139C>T (p.Pro380Leu) rs149136670
NM_052884.3(SIGLEC11):c.1281A>T (p.Gln427His) rs547243506
NM_052884.3(SIGLEC11):c.1291G>A (p.Glu431Lys) rs771866761
NM_052884.3(SIGLEC11):c.1304C>G (p.Thr435Ser) rs376222513
NM_052884.3(SIGLEC11):c.1304C>T (p.Thr435Ile) rs376222513
NM_052884.3(SIGLEC11):c.1339G>A (p.Val447Ile)
NM_052884.3(SIGLEC11):c.1339G>T (p.Val447Phe)
NM_052884.3(SIGLEC11):c.1357G>A (p.Val453Met)
NM_052884.3(SIGLEC11):c.1357G>C (p.Val453Leu)
NM_052884.3(SIGLEC11):c.1367C>T (p.Pro456Leu) rs765843318
NM_052884.3(SIGLEC11):c.1417T>C (p.Cys473Arg)
NM_052884.3(SIGLEC11):c.1448C>G (p.Pro483Arg) rs761548091
NM_052884.3(SIGLEC11):c.1451C>A (p.Ser484Tyr)
NM_052884.3(SIGLEC11):c.1457G>C (p.Arg486Pro) rs200767146
NM_052884.3(SIGLEC11):c.1457G>T (p.Arg486Leu)
NM_052884.3(SIGLEC11):c.154G>C (p.Val52Leu)
NM_052884.3(SIGLEC11):c.1562A>C (p.His521Pro) rs774700270
NM_052884.3(SIGLEC11):c.164A>G (p.Asn55Ser)
NM_052884.3(SIGLEC11):c.1702G>A (p.Gly568Ser)
NM_052884.3(SIGLEC11):c.1774C>T (p.Arg592Cys)
NM_052884.3(SIGLEC11):c.1775G>A (p.Arg592His)
NM_052884.3(SIGLEC11):c.1783G>A (p.Ala595Thr)
NM_052884.3(SIGLEC11):c.1973C>T (p.Ala658Val) rs201942673
NM_052884.3(SIGLEC11):c.2011A>G (p.Ile671Val)
NM_052884.3(SIGLEC11):c.2042G>A (p.Gly681Asp)
NM_052884.3(SIGLEC11):c.298C>T (p.Arg100Trp)
NM_052884.3(SIGLEC11):c.299G>A (p.Arg100Gln) rs769247998
NM_052884.3(SIGLEC11):c.317C>T (p.Thr106Ile) rs1192258338
NM_052884.3(SIGLEC11):c.324T>A (p.Asp108Glu) rs2514940017
NM_052884.3(SIGLEC11):c.328G>A (p.Gly110Ser)
NM_052884.3(SIGLEC11):c.373G>A (p.Asp125Asn) rs2076238604
NM_052884.3(SIGLEC11):c.403A>G (p.Arg135Gly)
NM_052884.3(SIGLEC11):c.412C>T (p.Arg138Cys)
NM_052884.3(SIGLEC11):c.437A>T (p.Asn146Ile)
NM_052884.3(SIGLEC11):c.514C>G (p.Pro172Ala) rs2514938327
NM_052884.3(SIGLEC11):c.574T>C (p.Ser192Pro)
NM_052884.3(SIGLEC11):c.68T>C (p.Leu23Pro)
NM_052884.3(SIGLEC11):c.727G>A (p.Val243Ile) rs1344155822
NM_052884.3(SIGLEC11):c.731G>A (p.Arg244Gln)
NM_052884.3(SIGLEC11):c.790T>A (p.Ser264Thr) rs1411027244
NM_052884.3(SIGLEC11):c.851G>A (p.Arg284Gln) rs773748696
NM_052884.3(SIGLEC11):c.979G>A (p.Gly327Arg)
NM_052884.3(SIGLEC11):c.992G>A (p.Arg331His) rs150164114

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.